Canonical Allele Identifier: CA576708067
Gene: ASNS HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97852480del , CM000669.2:g.97852480del GRCh38
NC_000007.13:g.97481792del , CM000669.1:g.97481792del GRCh37
NC_000007.12:g.97319728del NCBI36
NG_033870.1:g.25064del
NG_033870.2:g.81084del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394308.8:c.1477-11del MANE Select ENSP00000377845.3:n.1477-11del
ENST00000175506.8:c.1477-11del ENSP00000175506.4:n.1477-11del
ENST00000394308.7:c.1477-11del ENSP00000377845.3:n.1477-11del
ENST00000394309.7:c.1477-11del ENSP00000377846.3:n.1477-11del
ENST00000422745.5:c.1414-11del ENSP00000414901.1:n.1414-11del
ENST00000437628.5:c.1228-11del ENSP00000414379.1:n.1228-11del
ENST00000444334.5:c.1414-11del ENSP00000406994.1:n.1414-11del
ENST00000454046.5:c.*345-11del ENSP00000401651.1:n.*345-11del
ENST00000455086.5:c.1228-11del ENSP00000408472.1:n.1228-11del
ENST00000487714.1:n.535-11del
NM_001178075.1:c.1414-11del NP_001171546.1:n.1414-11del
NM_001178076.1:c.1228-11del NP_001171547.1:n.1228-11del
NM_001178077.1:c.1228-11del NP_001171548.1:n.1228-11del
NM_001673.4:c.1477-11del NP_001664.3:n.1477-11del
NM_133436.3:c.1477-11del NP_597680.2:n.1477-11del
NM_183356.3:c.1477-11del NP_899199.2:n.1477-11del
NM_001352496.1:c.1477-11del NP_001339425.1:n.1477-11del
NR_147989.1:n.3180-11del
NM_001673.5:c.1477-11del MANE Select NP_001664.3:n.1477-11del
NM_001178075.2:c.1414-11del NP_001171546.1:n.1414-11del
NM_001178076.2:c.1228-11del NP_001171547.1:n.1228-11del
NM_001352496.2:c.1477-11del NP_001339425.1:n.1477-11del
NM_183356.4:c.1477-11del NP_899199.2:n.1477-11del